FDA.reportPublic FDA data

Ear Dry

Manufacturer
Cardinal Health
Effective date
2011-01-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 01:47:11

Label at a glance#

ProductEar Dry Leader
Active ingredientIsopropyl Alcohol, Glycerin
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 94.998%, Glycerin 5.0%

INDICATIONS & USAGE SECTION

Uses

Helps relieves the discomfort of water-clogged ears by drying excess water due to water activities.

WARNINGS SECTION

Warnings

Do not use: if you have ear drainage or discharge, ear pain, irritation or rash in the ear, or are dizzy; consult a doctor.  If you have an injury or perforation (hole) of the ear drum of after ear surgery unless directed by a doctor.  Avoid contact with eyes.  If accidental contact occurs, flush eyes with water and consult a doctor. Discontinue use and consult a doctor if:  undue irritation or sensitivity occurs.

DOSAGE & ADMINISTRATION SECTION

Directions

FOR USE IN THE EAR ONLY.  To use:  remove cap, apply 4-5 drops in each ear after exposing ears to water such as swimming, showering or bathing or as directed by a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aloe Barbadensis Leaf Juice, Chamomile Recutita (Matricaria) Flower Oil.

OTC - PURPOSE SECTION

Purpose

Helps dry and relieve water-clogged ears.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ear Dry.

label imagelabel imagecarton imagecarton image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-617-102025-04-22C16284748780-19d75b9d0-c2e3-f424-e053-dadaa90a57ceDrug Facts
37205-617-102020-01-31C16284748780-19d75b9d0-c2e3-f424-e053-dadaa90a57ceDrug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-617-10ML - Milliliter37205-617884f4503-f2f9-4e45-8fc1-c36fa25e7f3c12014-04-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX4
Isopropyl AlcoholACTIVE INGREDIENTND2M4163024
GlycerinACTIVE MOIETYPDC6A3C0OX4
Isopropyl AlcoholACTIVE MOIETYND2M4163024
AloeINACTIVE INGREDIENTV5VD430YW94
ChamomileINACTIVE INGREDIENTFGL3685T2X4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37205-61737205-617-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
Isopropyl AlcoholND2M416302ACTIB
AloeV5VD430YW9IACT
ChamomileFGL3685T2XIACT
GlycerinPDC6A3C0OXACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3ca1f968-36c9-46a5-b7ce-4e6bf139b0b7cb566013-3fc4-4636-b214-3de64ce73b912025-04-16WarningsExact identifier
spl set id: cb566013-3fc4-4636-b214-3de64ce73b91

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.